e) 9-bromo 5-methyl 2-nonene -----H2, Ni 900°C---------- ? (name, str, stereochem) Cl2, CH2C12 f) cyclopentene ? (name, str, stereochem) CHOH g) ? (name, str, stereochem) -- hydroboration ----- achiral 3-methyl-1-butanol CH-CH

Chemistry
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ISBN:9781305957404
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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**Transcription for Educational Website:**

Predict the NAME, STRUCTURE, and STEREOCHEMISTRY of the BEST ORGANIC REACTANT or the MAJOR ORGANIC product for the following reactions:

(Note: There are no graphs or diagrams in the image to explain in detail.)
Transcribed Image Text:**Transcription for Educational Website:** Predict the NAME, STRUCTURE, and STEREOCHEMISTRY of the BEST ORGANIC REACTANT or the MAJOR ORGANIC product for the following reactions: (Note: There are no graphs or diagrams in the image to explain in detail.)
### Chemical Reactions and Stereochemistry

#### e) Reaction of 9-bromo 5-methyl 2-nonene

- **Reagents**: H₂, Ni at 900°C
- **Product**: ?
- **Details**: Provide the name, structure, and stereochemistry of the resulting product.

#### f) Halogenation of Cyclopentene

- **Reagent**: Cl₂ in CH₂Cl₂
- **Product**: ?
- **Details**: Determine the name, structure, and stereochemistry of the product.

#### g) Hydroboration Reaction

- **Initial Compound**: ?
- **Reaction Type**: Hydroboration
- **Product**: Achiral 3-methyl-1-butanol
  - **Structure Diagram**:
    ```
       CHOH
        |
      CH2
        |
     CH-CH2
       |
     CH3
    ```
- **Details**: Identify the name, structure, and stereochemistry of the starting material.

#### h) Oxidation with Cold Dilute KMnO₄

- **Initial Compound**: ?
- **Reaction**: Cold dilute KMnO₄
- **Product**: (±) Erythro pentane 2,3-diol
  - **Structure Diagram**:
    ```
      CH3
       |
      H-C-OH
       |
      H-C-OH
       |
     CH2CH2
    ``` 
- **Details**: Establish the name, structure, and stereochemistry of the reacting compound.

#### i) Ozonolysis Reaction

- **Initial Compound**: ?
- **Reagents**: O₃, (CH₃)₂S
- **Product**: CH₃CH₂CHO
- **Details**: Confirm the name, structure, and stereochemistry of the starting alkene or compound.

Each reaction above should involve analysis and determination of the product's name, chemical structure, and stereochemical configuration.
Transcribed Image Text:### Chemical Reactions and Stereochemistry #### e) Reaction of 9-bromo 5-methyl 2-nonene - **Reagents**: H₂, Ni at 900°C - **Product**: ? - **Details**: Provide the name, structure, and stereochemistry of the resulting product. #### f) Halogenation of Cyclopentene - **Reagent**: Cl₂ in CH₂Cl₂ - **Product**: ? - **Details**: Determine the name, structure, and stereochemistry of the product. #### g) Hydroboration Reaction - **Initial Compound**: ? - **Reaction Type**: Hydroboration - **Product**: Achiral 3-methyl-1-butanol - **Structure Diagram**: ``` CHOH | CH2 | CH-CH2 | CH3 ``` - **Details**: Identify the name, structure, and stereochemistry of the starting material. #### h) Oxidation with Cold Dilute KMnO₄ - **Initial Compound**: ? - **Reaction**: Cold dilute KMnO₄ - **Product**: (±) Erythro pentane 2,3-diol - **Structure Diagram**: ``` CH3 | H-C-OH | H-C-OH | CH2CH2 ``` - **Details**: Establish the name, structure, and stereochemistry of the reacting compound. #### i) Ozonolysis Reaction - **Initial Compound**: ? - **Reagents**: O₃, (CH₃)₂S - **Product**: CH₃CH₂CHO - **Details**: Confirm the name, structure, and stereochemistry of the starting alkene or compound. Each reaction above should involve analysis and determination of the product's name, chemical structure, and stereochemical configuration.
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